U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 290

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138931copy number variation1nstd232human GRCh37.p13 chr2: 11,253,517-11,253,572 , GRCh38.p12 chr2: 11,113,391-11,113,446 FLJ33534
    nsv7138097copy number variation1nstd232human GRCh37.p13 chr2: 11,253,662-11,253,712 , GRCh38.p12 chr2: 11,113,536-11,113,586 FLJ33534
    nsv7048729inversion1nstd229human GRCh38 chr2: 10,950,861-12,841,358 , GRCh37.p13 chr2: 11,090,987-12,981,484 LOC101929752, LOC105373431, 34 more genes
    nsv6675366copy number variation1nstd229human GRCh38 chr2: 11,105,587-11,110,732 , GRCh37.p13 chr2: 11,245,713-11,250,858 FLJ33534
    nsv6669169copy number variation1nstd229human GRCh38 chr2: 11,129,201-11,135,600 , GRCh37.p13 chr2: 11,269,327-11,275,726 FLJ33534, C2orf50
    nsv6668755copy number variation1nstd229human GRCh38 chr2: 11,098,217-11,104,296 , GRCh37.p13 chr2: 11,238,343-11,244,422 RPL6P4, FLJ33534
    nsv6668308copy number variation1nstd229human GRCh38 chr2: 11,128,114-11,136,457 , GRCh37.p13 chr2: 11,268,240-11,276,583 FLJ33534, C2orf50
    nsv6667974copy number variation1nstd229human GRCh38 chr2: 11,108,301-11,116,300 , GRCh37.p13 chr2: 11,248,427-11,256,426 FLJ33534
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6664647copy number variation1nstd229human GRCh38 chr2: 11,124,101-11,145,900 , GRCh37.p13 chr2: 11,264,227-11,286,026 FLJ33534, C2orf50
    nsv6662499copy number variation1nstd229human GRCh38 chr2: 10,913,620-11,157,722 , GRCh37.p13 chr2: 11,053,746-11,297,848 KCNF1, C2orf50, 3 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6552342inversion1nstd223human GRCh38 chr2: 11,112,958-11,113,308 , GRCh37.p13 chr2: 11,253,084-11,253,434 FLJ33534
    nsv6336738copy number variation1nstd223human GRCh38 chr2: 11,108,576-11,108,799 , GRCh37.p13 chr2: 11,248,702-11,248,925 FLJ33534
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6297223copy number variation1nstd186human GRCh37 chr2: 11,246,348-11,247,401 , GRCh38.p12 chr2: 11,106,222-11,107,275 FLJ33534
    nsv6290643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 8,935,077-15,722,794 , GRCh38.p12 chr2: 8,794,947-15,582,670 PPIAP60, LOC105373431, 95 more genes
    nsv6290363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,717,186-12,013,065 , GRCh38.p12 chr2: 9,577,057-11,872,939 RNU4-73P, CYS1, 56 more genes
    nsv6261344copy number variation1nstd214human GRCh38 chr2: 11,113,428-11,113,483 , GRCh37.p13 chr2: 11,253,554-11,253,609 FLJ33534
    nsv6165734copy number variation1nstd214human GRCh38 chr2: 11,113,391-11,113,446 , GRCh37.p13 chr2: 11,253,517-11,253,572 FLJ33534
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center